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New study aims to better detect breathing trouble in Non-Communicative ICU patients

NCT ID NCT07383389

Knowledge-focused Sponsor: Istinye University Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study checks if a Turkish version of the Respiratory Distress Observation Scale (RDOS) accurately measures breathing distress in critically ill patients who cannot speak. Researchers will compare RDOS scores with end-tidal carbon dioxide levels, an objective breathing measure, in 64 ICU adults. The goal is to improve symptom monitoring and care for patients unable to report their own discomfort.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 64 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Feb 2026

An estimate. Start dates often move.

Expected to finish

Oct 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study population consists of adult patients aged 18 to 85 years who are hospitalized in the intensive care unit with clinically diagnosed dyspnea and underlying cardiopulmonary or systemic conditions. Eligible participants are patients who are unable to reliably self-report respiratory distress due to critical illness or impaired communication. Patients who are fully dependent on mechanical ventilation or have severe central nervous system disorders affecting respiratory control are excluded.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Being 18 years of age or older, * Having a diagnosis of lung or pleural cancer, chronic kidney failure, congestive heart failure, COPD, asthma, or pneumonia presenting with dyspnea, * Being specifically referred for treatment of dyspnea, * Having been in the intensive care unit for at least one day, * Participation in the study must be consented to by the individual or a family member. Exclusion Criteria: * Being completely ventilator-dependent, * Having a diagnosis of central nervous system disease (quadriplegia, bulbar ALS).

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Conditions

The condition(s) this trial relates to.

asthma chronic obstructive pulmonary disease chronic renal failure syndrome congestive heart failure Critical Illness lung cancer pleural cancer pneumonia

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Critical care, intensive care Critical illness

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  2. A doctor treating you

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More trials for these conditions

Other studies related to the condition(s) this trial covers.